Canonical Allele Identifier: CA1310518881

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178533958A= , CM000664.2:g.178533958A= GRCh38
NC_000002.11:g.179398685A= , CM000664.1:g.179398685A= GRCh37
NC_000002.10:g.179106931A= NCBI36
NG_011618.3:g.301845T= , LRG_391:g.301845T=
NG_051363.1:g.16132A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.94953T= (TTN) ENSP00000343764.6:p.Ser31651=
ENST00000342175.11:c.76038T= (TTN) ENSP00000340554.6:p.Ser25346=
ENST00000359218.10:c.75837T= (TTN) ENSP00000352154.5:p.Ser25279=
ENST00000342175.10:c.76038T= (TTN) ENSP00000340554.6:p.Ser25346=
ENST00000342992.10:c.94953T= (TTN) ENSP00000343764.6:p.Ser31651=
ENST00000359218.9:c.75837T= (TTN) ENSP00000352154.5:p.Ser25279=
ENST00000460472.6:c.75462T= (TTN) ENSP00000434586.1:p.Ser25154=
ENST00000589042.5:c.102657T= (TTN) MANE Select ENSP00000467141.1:p.Ser34219=
ENST00000591111.5:c.97734T= (TTN) ENSP00000465570.1:p.Ser32578=
ENST00000615779.4:c.97734T= (TTN) ENSP00000483597.1:p.Ser32578=
NM_001256850.1:c.97734T= (TTN) NP_001243779.1:p.Ser32578=
NM_001267550.2:c.102657T= (TTN) MANE Select NP_001254479.2:p.Ser34219=
NM_003319.4:c.75462T= (TTN) NP_003310.4:p.Ser25154=
NM_133378.4:c.94953T= (TTN) NP_596869.4:p.Ser31651=
NM_133432.3:c.75837T= (TTN) NP_597676.3:p.Ser25279=
NM_133437.4:c.76038T= (TTN) NP_597681.4:p.Ser25346=
NR_038271.1:n.446+10322A= (TTN-AS1)
NR_038272.1:n.220-1774A= (TTN-AS1)
XM_011511729.1:c.101754T= (TTN) XP_011510031.1:p.Ser33918=
XM_011511730.1:c.75648T= (TTN) XP_011510032.1:p.Ser25216=
XM_011511731.1:c.75507T= (TTN) XP_011510033.1:p.Ser25169=
XM_017004819.1:c.101550T= (TTN) XP_016860308.1:p.Ser33850=
XM_017004820.1:c.96948T= (TTN) XP_016860309.1:p.Ser32316=
XM_017004821.1:c.96945T= (TTN) XP_016860310.1:p.Ser32315=
XM_017004822.1:c.93987T= (TTN) XP_016860311.1:p.Ser31329=
XM_017004823.1:c.75603T= (TTN) XP_016860312.1:p.Ser25201=
XM_024453094.1:c.97098T= (TTN) XP_024308862.1:p.Ser32366=
XM_024453095.1:c.97095T= (TTN) XP_024308863.1:p.Ser32365=
XM_024453096.1:c.96528T= (TTN) XP_024308864.1:p.Ser32176=
XM_024453097.1:c.93870T= (TTN) XP_024308865.1:p.Ser31290=
XM_024453098.1:c.93789T= (TTN) XP_024308866.1:p.Ser31263=
XM_024453099.1:c.75552T= (TTN) XP_024308867.1:p.Ser25184=
XM_024453100.1:c.65406T= (TTN) XP_024308868.1:p.Ser21802=